HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → Ethyl 3-[4-(2-methoxyphenyl)piperazino]propanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 3-bromopropionate | HCID 68320 | — |
| Reactant | N-(2-Methoxyphenyl)piperazine hydrochloride | HCID 9899402 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ethyl 3-[4-(2-methoxyphenyl)piperazino]propanoate | HCID 12234156 | 71.4% |
Reaction Steps
A mixture of 1-(2-methoxyphenyl)piperazine hydrochloride (9.10 g, 39.78 mmol), ethyl 3-bromopropionate (7.29 g, 5.14 mL, 40.29 mmol), potassium carbonate (20.00 g, 144.70 mmol) and a catalytic amount of potassium iodide in acetonitrile (80 mL) was heated at reflux for 18 hrs. After cooling at room temperature the solvent was evaporated under reduced pressure and the residue was taken up in dichloromethane. The organic phase was washed with water, dried over MgSO4 and evaporated to dryness. The resulting orange oil was purified by flash chromatography (Silica gel 60 Å, 45 μm, 50% ethyl acetate in hexane) and afforded 8.30 g (71%) ethyl 3-[4-(2-methoxyphenyl)piperazino]propanoate D1 as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08222254B2 |
| Source dataset | uspto-grants-2012_07 |
| ORD ID | ord-a7b7cc57764947beb1bd628dfede1751 |
| Source note | uspto-grants-2012_07 |